Clinical Research Associate - Maseeraty Graduate Program, UAE
Dubai, Dubai, UAE/Dubai
Listed on 2026-01-12
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Science
Clinical Research
"Clinical Research Associate – Maseeraty Graduate Program, UAE
Emirati Graduate Program Associate (Fixed Term Contract). We are welcoming UAE National Talents to apply for our Novartis Emiratization Program, a 12‑month program that provides real‑world experience to apply theoretical learning to practice.
Program highlights:
- Thorough onboarding and understanding of Novartis functions, including Sales & Marketing, Medical, Value & Access and support functions.
- Participation and leadership of key projects across the organization.
- Development of management skills.
Successful completion gives Emirati talents the opportunity to apply to permanent roles within the organization.
Eligibility:
If you are a UAE National, hold a UAE Family Book and have obtained a Bachelor’s Degree within the past 3 years, and are passionate about joining an organization that promotes an unbossed, diverse and flexible working environment, hurry and apply.
The Clinical Research Associate role involves company training to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, GCP, ICH guidelines, local regulations and Novartis SOPs. Responsibilities include delivering data within timelines and required quality standard.
Major Activities- Complete appropriate Gen Med and project‑specific training, including therapeutic, protocol and clinical research training.
- Gain experience in study procedures by working with Clinical Research Associate (CRA) and Clinical Operation Lead (COL) roles.
- Gain knowledge and experience on site selection, initiation, monitoring and close‑out visits in accordance with contracted scope and GCP.
- Support local CRA in training sites on study protocol, establish regular communication lines, and manage project expectations and issues.
- Support local CRA in evaluating the quality and integrity of site practices, casting quality issues to COL.
- Assist in managing the progress of assigned studies, including regulatory submissions, approvals, recruitment and enrollment.
- Track trial execution milestones, identify problems, resolve issues and appropriately escalates.
- Under close supervision, facilitate preparation and archival of study documents.
- Training on RWE activities.
- Training on processes: SOPs, WPs, guidance.
- Accompany CRA for site selection and initiation visits.
- Study management system training and access.
- TMF maintenance and archival on electronic document management systems.
- Support in preparing study submission package.
- We are a diverse group of 200+ associates across the Gulf region, with more than 30 nationalities.
- We offer flexible working conditions with a hybrid working model allowing work from home during the week.
- We provide an inspired, curious and unbossed working environment led with integrity.
- We promote personal growth and career development opportunities.
Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other to achieve breakthroughs that change patients’ lives.
Benefits and RewardsRead our handbook to learn about all the ways we’ll help you thrive personally and professionally:
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